Umbelliferone (BioDeep_00000000007)
Secondary id: BioDeep_00000400511, BioDeep_00000422454, BioDeep_00000861538
human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite
代谢物信息卡片
化学式: C9H6O3 (162.03169259999999)
中文名称: 7-羟基香豆素
谱图信息:
最多检出来源 Homo sapiens(blood) 0.01%
Last reviewed on 2024-07-12.
Cite this Page
Umbelliferone. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/umbelliferone (retrieved
2024-09-08) (BioDeep RN: BioDeep_00000000007). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: C1=CC(=CC2=C1C=CC(=O)O2)O
InChI: InChI=1S/C9H6O3/c10-7-3-1-6-2-4-9(11)12-8(6)5-7/h1-5,10H
描述信息
Umbelliferone is a hydroxycoumarin that is coumarin substituted by a hydroxy group ay position 7. It has a role as a fluorescent probe, a plant metabolite and a food component.
Umbelliferone is a natural product found in Ficus septica, Artemisia ordosica, and other organisms with data available.
See also: Chamomile (part of).
Occurs widely in plants including Angelica subspecies Phytoalexin of infected sweet potato. Umbelliferone is found in many foods, some of which are macadamia nut, silver linden, quince, and capers.
Umbelliferone is found in anise. Umbelliferone occurs widely in plants including Angelica species Phytoalexin of infected sweet potat
A hydroxycoumarin that is coumarin substituted by a hydroxy group ay position 7.
[Raw Data] CB220_Umbelliferone_pos_50eV_CB000077.txt
[Raw Data] CB220_Umbelliferone_pos_40eV_CB000077.txt
[Raw Data] CB220_Umbelliferone_pos_30eV_CB000077.txt
[Raw Data] CB220_Umbelliferone_pos_10eV_CB000077.txt
[Raw Data] CB220_Umbelliferone_pos_20eV_CB000077.txt
[Raw Data] CB220_Umbelliferone_neg_40eV_000039.txt
[Raw Data] CB220_Umbelliferone_neg_10eV_000039.txt
[Raw Data] CB220_Umbelliferone_neg_30eV_000039.txt
[Raw Data] CB220_Umbelliferone_neg_20eV_000039.txt
Umbelliferone. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=93-35-6 (retrieved 2024-07-12) (CAS RN: 93-35-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Umbelliferone (7-Hydroxycoumarin), a natural product of the coumarin family, is a fluorescing compound which can be used as a sunscreen agent.
Umbelliferone (7-Hydroxycoumarin), a natural product of the coumarin family, is a fluorescing compound which can be used as a sunscreen agent.
同义名列表
66 个代谢物同义名
Umbelliferone; Umbelliferone, suitable for fluorescence indicator, >=98.0\\% (HPLC); InChI=1/C9H6O3/c10-7-3-1-6-2-4-9(11)12-8(6)5-7/h1-5,10; Umbelliferone, Vetec(TM) reagent grade, 98\\%; 5-18-01-00386 (Beilstein Handbook Reference); 7-Hydroxycoumarin;Hydrangin;NSC 19790; Umbelliferone (Hydrangin, Skimmetin); Umbelliferone, analytical standard; 2H-1-Benzopyran-2-one, 7-hydroxy-; 7-Hydroxy-2H-1-benzopyran-2-one; 7-hydroxycoumarin, 14C-labeled; 7-Hydroxy-2H-chromen-2-one #; 7-hydroxy-1-benzopyran-2-one; 7-Hydroxy-2H-chromen-2-one; 7-hydroxycoumarin sulphate; 2-Hydroxy-7H-chromen-7-one; 7-hydroxycoumarin sulfate; Coumarin derivative, 3a; 7-Hydroxy Coumarin ,(S); 7-oxidanylchromen-2-one; 7-hydroxy-chromen-2-one; 7-hydroxychromen-2-one; UMBELLIFERONE [WHO-DD]; 7-Hydroxy-2-chromenone; .beta.-Umbelliferone; Coumarin, 7-hydroxy-; beta -umbelliferone; Umbelliferone, 99\\%; 7-hydroxy-coumarine; 7-hydroxycournarin; 7-hydroxy-coumarin; 7-hydroxycoumarine; 7-hydroxy coumarin; beta-Umbelliferone; UMBELLIFERONE [MI]; 7-Hydroxycoumarin; Spectrum3_000751; Spectrum2_001962; 7-hydroxycumarin; UNII-60Z60NTL4G; b-Umbelliferone; Β-umbelliferone; 7 OH COUMARIN; Umbelliferone; MEGxp0_000814; 7-Oxycoumarin; NCI60_001646; ACon1_000219; KBio3_001582; Umbelliferon; 60Z60NTL4G; Hydrangine; Skimmetine; Dichrin A; Skimmetin; Hydrangin; AI3-38054; 1ST11436; 7-HC; 7 HC; 07L; 7-Hydroxy-2H-1-benzopyran-2-one; 7-Oxycoumarin; Skimmetin; Hydrangin; NSC 19790
数据库引用编号
50 个数据库交叉引用编号
- ChEBI: CHEBI:27510
- KEGG: C09315
- PubChem: 5281426
- HMDB: HMDB0029865
- Metlin: METLIN44642
- ChEMBL: CHEMBL51628
- Wikipedia: Umbelliferone
- MeSH: 7-hydroxycoumarin
- ChemIDplus: 0000093356
- MetaCyc: CPD-8186
- KNApSAcK: C00002503
- foodb: FDB001094
- chemspider: 4444774
- CAS: 93-35-6
- MoNA: FIO00499
- MoNA: NA003261
- MoNA: NA003259
- MoNA: NA002487
- MoNA: FIO00497
- MoNA: NA003624
- MoNA: NA002881
- MoNA: NA002883
- MoNA: NA003626
- MoNA: NA003260
- MoNA: FIO00500
- MoNA: NA002880
- MoNA: NA003627
- MoNA: NA002486
- MoNA: NA002489
- MoNA: FIO00501
- MoNA: FIO00495
- MoNA: FIO00493
- MoNA: NA003625
- MoNA: NA002879
- MoNA: NA003628
- MoNA: NA003263
- MoNA: NA002490
- MoNA: FIO00494
- MoNA: NA002882
- MoNA: FIO00498
- MoNA: NA003262
- MoNA: FIO00496
- MoNA: NA002488
- PMhub: MS000000957
- MetaboLights: MTBLC27510
- PDB-CCD: 07L
- 3DMET: B02855
- NIKKAJI: J4.673F
- RefMet: Umbelliferone
- medchemexpress: HY-N0573
分类词条
相关代谢途径
Reactome(5)
BioCyc(7)
PlantCyc(6)
代谢反应
624 个相关的代谢反应过程信息。
Reactome(55)
- Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA
- Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Cytochrome P450 - arranged by substrate type:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Xenobiotics:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN
- Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA
- Biological oxidations:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN
- Phase I - Functionalization of compounds:
CH3CHO + H2O + NAD ⟶ CH3COO- + H+ + NADH
- Cytochrome P450 - arranged by substrate type:
ANDST + H+ + Oxygen + TPNH ⟶ H2O + HCOOH + TPN + estrone
- Xenobiotics:
EtOH + H+ + Oxygen + TPNH ⟶ CH3CHO + H2O + TPN
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Cytochrome P450 - arranged by substrate type:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Xenobiotics:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Cytochrome P450 - arranged by substrate type:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Xenobiotics:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN
- Metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi
- Biological oxidations:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN
- Phase I - Functionalization of compounds:
CH3CHO + H2O + NAD ⟶ CH3COO- + H+ + NADH
- Cytochrome P450 - arranged by substrate type:
EtOH + H+ + Oxygen + TPNH ⟶ CH3CHO + H2O + TPN
- Xenobiotics:
EtOH + H+ + Oxygen + TPNH ⟶ CH3CHO + H2O + TPN
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Biological oxidations:
CH3CHO + H2O + NAD ⟶ CH3COO- + H+ + NADH
- Phase I - Functionalization of compounds:
CH3CHO + H2O + NAD ⟶ CH3COO- + H+ + NADH
- Cytochrome P450 - arranged by substrate type:
ANDST + H+ + Oxygen + TPNH ⟶ H2O + HCOOH + TPN + estrone
- Xenobiotics:
DEXM + H+ + Oxygen + TPNH ⟶ CH2O + DEXT + H2O + TPN
- Metabolism:
3alpha,7alpha,12alpha-trihydroxy-5beta-cholest-24-one-CoA + CoA-SH ⟶ choloyl-CoA + propionyl CoA
- Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Cytochrome P450 - arranged by substrate type:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Xenobiotics:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Cytochrome P450 - arranged by substrate type:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Xenobiotics:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN
- Metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA
- Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Cytochrome P450 - arranged by substrate type:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Xenobiotics:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN
- Metabolism:
ATP + PROP-CoA + carbon dioxide ⟶ ADP + MEMA-CoA + Pi
- Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Cytochrome P450 - arranged by substrate type:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Xenobiotics:
CAF + H+ + Oxygen + TPNH ⟶ CH2O + H2O + Paraxanthine + TPN
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Biological oxidations:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Phase I - Functionalization of compounds:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Cytochrome P450 - arranged by substrate type:
11DCORT + H+ + Oxygen + TPNH ⟶ CORT + H2O + TPN
- Xenobiotics:
H+ + Oxygen + TPNH + aflatoxin B1 ⟶ AFXBO + H2O + TPN
BioCyc(8)
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- coumarins biosynthesis (engineered):
6'-hydroxyferuloyl-CoA ⟶ coenzyme A + scopoletin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
(Z)-6'-hydroxyferulate ⟶ scopoletin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
SAM + esculetin ⟶ H+ + SAH + scopoletin
- simple coumarins biosynthesis:
scopoletin ⟶ a demethylated methyl donor + scoparone
- coumarins biosynthesis (engineered):
6'-hydroxyferuloyl-CoA ⟶ coenzyme A + scopoletin
WikiPathways(0)
Plant Reactome(246)
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
DMAPP + genistein ⟶ PPi + lupiwighteone
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate
- Secondary metabolism:
DMAPP + genistein ⟶ PPi + lupiwighteone
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
DMAPP + genistein ⟶ PPi + lupiwighteone
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate
- Secondary metabolism:
DMAPP + genistein ⟶ PPi + lupiwighteone
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate
- Secondary metabolism:
DMAPP + genistein ⟶ PPi + lupiwighteone
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
L-Phe ⟶ ammonia + trans-cinnamate
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
L-Glu + imidazole acetol-phosphate ⟶ 2OG + L-histidinol-phosphate
- Secondary metabolism:
Fru(6)P + L-Gln ⟶ GlcN6P + L-Glu
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
FAD + PROP-CoA ⟶ FADH2 + acryloyl-CoA
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
ATP + CoA + propionate ⟶ AMP + PPi + PROP-CoA
- Secondary metabolism:
GPP + H2O ⟶ PPi + geraniol
- Linear furanocoumarin biosynthesis:
H+ + H2O + TPNH + psoralen ⟶ TPN + bergaptol
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
- Metabolism and regulation:
CoA + NAD + methylmalonate-semialdehyde ⟶ NADH + PROP-CoA + carbon dioxide
- Secondary metabolism:
ATP + CoA-SH + ferulate ⟶ AMP + PPi + feruloyl-CoA
- Linear furanocoumarin biosynthesis:
DMAPP + HCOU ⟶ PPi + demethylsuberosin
INOH(0)
PlantCyc(315)
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
H+ + NADPH + O2 + psoralen ⟶ H2O + NADP+ + bergaptol
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- coumarins biosynthesis (engineered):
trans-6-hydroxyferuloyl-CoA ⟶ coenzyme A + scopoletin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
(Z)-6'-hydroxyferulate ⟶ scopoletin
- simple coumarins biosynthesis:
scopoletin ⟶ a demethylated methyl donor + scoparone
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2-oxoglutarate + 4-coumaroyl-CoA + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + H+ + NADPH + O2 ⟶ H2O + NADP+ + acetone + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2-oxoglutarate + 4-coumaroyl-CoA + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + H+ + NADPH + O2 ⟶ H2O + NADP+ + acetone + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
(E)-4-coumaroyl-CoA + 2-oxoglutarate + O2 ⟶ 2,4-dihydroxycinnamoyl-CoA + CO2 + succinate
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + H+ + NADPH + O2 ⟶ H2O + NADP+ + acetone + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- simplecoumarins biosynthesis:
5-O-caffeoylshikimate ⟶ caffeate
- coumarins biosynthesis (engineered):
trans-6-hydroxyferuloyl-CoA ⟶ coenzyme A + scopoletin
- superpathway of scopolin and esculin biosynthesis:
(Z)-6'-hydroxyferulate ⟶ scopoletin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- coumarins biosynthesis (engineered):
trans-6-hydroxyferuloyl-CoA ⟶ coenzyme A + scopoletin
- superpathway of scopolin and esculin biosynthesis:
UDP-α-D-glucose + scopoletin ⟶ H+ + UDP + scopolin
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- umbelliferone biosynthesis:
2,4-dihydroxycinnamoyl-CoA ⟶ coenzyme A + umbelliferone
- linear furanocoumarin biosynthesis:
(+)-marmesin + O2 + a reduced [NADPH-hemoprotein reductase] ⟶ H2O + acetone + an oxidized [NADPH-hemoprotein reductase] + psoralen
- superpathway of scopolin and esculin biosynthesis:
H2O + esculin ⟶ D-glucopyranose + esculetin
- linear furanocoumarin biosynthesis:
H+ + NADPH + O2 + psoralen ⟶ H2O + NADP+ + bergaptol
- linear furanocoumarin biosynthesis:
H+ + NADPH + O2 + psoralen ⟶ H2O + NADP+ + bergaptol
- umbelliferone biosynthesis:
4-coumarate + ATP + coenzyme A ⟶ (E)-4-coumaroyl-CoA + AMP + diphosphate
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680 个相关的物种来源信息
- 33090 金盏花: -
- 3498 桑叶: -
- 9606 Homo sapiens:
- 142738 Stellera chamaejasme:
- 68554 Phellodendron amurense:
- 159071 Zanthoxylum ailanthoides:
- 76967 Glycosmis pentaphylla:
- 43711 Murraya paniculata:
- 2901850 Murraya exotica:
- 354522 Tetradium glabrifolium:
- 880079 Rhododendron dauricum: 10.1007/S10600-010-9649-7
- 354509 Phellodendron chinense var. glabriusculum: 10.1021/NP030034V
- 697203 Phellodendron amurense var. wilsonii: 10.1021/NP030034V
- 2099548 Zanthoxylum zanthoxyloides: 10.1021/NP50046A035
- 98504 Matricaria chamomilla:
- 115623 Herniaria: 10.1007/BF00566073
- 3039 Euglena gracilis: 10.3389/FBIOE.2021.662655
- 1227633 Artemisia minor:
- 237931 Viburnum cylindricum: 10.1002/HLCA.200800420
- 669127 Artemisia lactiflora: 10.4268/CJCMM20141334
- 1056465 Zanthoxylum beecheyanum: 10.1002/JCCS.200400159
- 216479 Euphorbia maculata: 10.4268/CJCMM20141227
- 216481 Euphorbia nutans: 10.4268/CJCMM20141227
- 29760 Vitis vinifera: 10.1002/JSSC.200500003
- 53873 Dipteryx odorata: 10.1021/JF00111A051
- 4047 Coriandrum sativum: 10.1016/0031-9422(95)00930-2
- 97171 Abies nephrolepis: 10.1002/CBDV.201000373
- 210328 Maclura tricuspidata: 10.3987/COM-90-5416
- 1435564 Kalanchoe laciniata: 10.1021/NP50065A009
- 1091133 Astragalus onobrychis: 10.1007/BF00630446
- 203000 Rhodiola sacra: 10.1007/BF00564830
- 237933 Viburnum dilatatum: 10.1016/0031-9422(95)00790-3
- 1264805 Astragalus brachycarpus: 10.1007/BF00564977
- 100580 Ficus virens: 10.1016/J.JEP.2008.06.025
- 3494 Ficus carica: 10.1016/J.JEP.2008.06.025
- 549434 Zanthoxylum rhoifolium:
- 1968 Streptomyces cellulosae: 10.1186/S12906-018-2154-4
- 46147 Portulaca oleracea: 10.1002/HLCA.201000250
- 125587 Bistorta officinalis: 10.4268/CJCMM20161721
- 254780 Persicaria amphibia: 10.4268/CJCMM20161721
- 157791 Vigna radiata: 10.1007/BF00598601
- 3916 Vigna radiata var. radiata: 10.1007/BF00598601
- 3885 Phaseolus vulgaris:
- 53861 Securigera varia:
- 181251 Securigera elegans:
- 390705 Securigera securidaca: 10.1007/BF00598775
- 203004 Rhodiola heterodonta: 10.1007/BF00564822
- 1279044 Melilotus messanensis: 10.1055/S-0028-1097913
- 200951 Melilotus indicus: 10.1055/S-0028-1097913
- 195662 Prunus prostrata: 10.1021/NP50102A017
- 428217 Callisia fragrans: 10.1007/S10600-009-9174-8
- 212301 Euphorbia humifusa: 10.1016/J.BMCL.2014.03.014
- 91096 Hylotelephium ewersii: 10.1007/BF00567817
- 2816892 Heteroplexis microcephala: 10.1021/NP900213W
- 35883 Ipomoea nil:
- 487764 Rhodiola quadrifida: 10.1007/BF00563908
- 1442767 Rhodiola coccinea: 10.1007/BF00563908
- 182159 Rhododendron spinuliferum: 10.1007/S10600-009-9410-2
- 626692 Caragana spinosa: 10.1007/S10600-012-0124-5
- 72349 Artemisia nova: 10.1016/S0021-9673(01)97678-2
- 55611 Artemisia tridentata:
- 187461 Chamaecyparis formosensis: 10.1016/S0031-9422(99)00074-6
- 1441046 Lomatia hirsuta: 10.1016/S0378-8741(97)00048-2
- 4222 Carthamus tinctorius: 10.1023/B:CONC.0000025456.09089.84
- 85712 Angelica gigas:
- 48101 Angelica dahurica:
- 357970 Angelica biserrata:
- 312530 Angelica pubescens:
- 369397 Picea neoveitchii: 10.1016/J.PHYTOCHEM.2011.01.018
- 33117 Mandragora officinarum: 10.1016/J.PHYTOCHEM.2005.07.016
- 389206 Mandragora autumnalis: 10.1016/J.PHYTOCHEM.2005.07.016
- 100573 Ficus septica: 10.3987/COM-02-9615
- 1745051 Disynaphia multicrenulata: 10.1016/S0031-9422(00)80481-1
- 573714 Baccharis trinervis: 10.1016/S0031-9422(00)80758-X
- 354517 Skimmia reevesiana: 10.1016/S0031-9422(00)84814-1
- 23278 Vahlia capensis: 10.1016/0031-9422(94)00710-B
- 1227617 Artemisia assoana: 10.1016/S0031-9422(00)83891-1
- 72339 Artemisia chamaemelifolia:
- 205376 Artemisia santolinifolia:
- 401898 Artemisia gmelinii:
- 392618 Cunila: 10.1007/S00299-018-2303-8
- 205371 Artemisia marschalliana: 10.1016/S0031-9422(00)88402-2
- 224035 Daphne oleoides:
- 329675 Daphne odora:
- 1619493 Melicope hayesii: 10.1016/S0031-9422(98)00720-1
- 23110 Hydrangea macrophylla:
- 859264 Hydrangea serrata: 10.1248/CPB.40.3121
- 1811969 Artemisia vestita: 10.1055/S-1999-13965
- 2753872 Daphne acutiloba: 10.1016/S0031-9422(98)00181-2
- 66680 Daphne mezereum:
- 224084 Wikstroemia canescens: 10.1248/CPB.60.554
- 669133 Artemisia mongolica: 10.1055/S-2006-957946
- 88733 Pinus armandii:
- 2753873 Daphne feddei: 10.1080/10286020.2011.621892
- 885948 Daphne tangutica: 10.1016/J.FITOTE.2009.07.002
- 347984 Coronilla viminalis:
- 390707 Coronilla vaginalis:
- 66391 Fatoua villosa: 10.1002/CBDV.200900326
- 241879 Fatoua pilosa: 10.1002/CBDV.200900326
- 118892 Coronilla scorpioides:
- 52496 Prangos: 10.1007/BF00781092
- 48026 Ammi majus:
- 325744 Prangos uloptera: 10.1248/CPB.49.877
- 1585712 Prangos tschimganica: 10.1248/CPB.49.877
- 463862 Ficus nervosa: 10.1002/CBDV.200900227
- 282648 Asterolasia phebalioides: 10.1016/0305-1978(94)90036-1
- 1090619 Ayapana triplinervis: 10.1016/0031-9422(71)85045-8
- 171251 Citrus medica:
- 549427 Metrodorea nigra: 10.1016/0031-9422(95)00504-Z
- 265806 Angelica japonica: 10.1248/CPB.29.2565
- 142181 Edgeworthia chrysantha:
- 883867 Matricaria discoidea: 10.1007/BF00579084
- 56017 Matricaria matricarioides: 10.1007/BF00579084
- 43493 Haldina cordifolia:
- 169606 Tagetes lucida: 10.1021/JF053071W
- 401909 Artemisia laciniata: 10.1002/JLAC.198619861208
- 2567738 Yponomeuta padella: 10.1007/BF01041730
- 263927 Yponomeuta mahalebellus: 10.1007/BF01041730
- 129217 Prunus mahaleb: 10.1007/BF01041730
- 860753 Hydrangea heteromalla:
- 52833 Hydrangea paniculata:
- 498914 Hydrangea chinensis:
- 489434 Prangos ferulacea: 10.1590/S0102-695X2008000100002
- 118509 Glebionis segetum:
- 380075 Heracleum grandiflorum: 10.1007/BF02249699
- 380073 Heracleum dissectum: 10.1007/S11418-008-0266-8
- 99506 Heracleum candicans: 10.1007/S11418-008-0266-8
- 282612 Nematolepis squamea: 10.1016/0031-9422(92)83450-D
- 282620 Rhadinothamnus anceps: 10.1016/0031-9422(92)83450-D
- 282633 Phebalium squamulosum:
- 357850 Angelica keiskei: 10.1016/0031-9422(90)85357-L
- 68527 Aegle marmelos:
- 77053 Pleiospermium alatum:
- 446321 Althaea armeniaca: 10.1007/BF00630189
- 145745 Althaea officinalis: 10.1007/BF00630189
- 714449 Artemisia anomala: 10.1016/S0031-9422(00)83589-X
- 298346 Dictamnus albus:
- 217505 Sinacalia tangutica:
- 1044962 Rhododendron lepidotum: 10.1016/J.CCLET.2009.11.015
- 2715869 Daphne papyracea: 10.1248/CPB.34.595
- 2783874 Daphne mucronata:
- 202097 Scapholeberis mucronata:
- 546994 Daphne bholua: 10.1016/S0367-326X(99)00010-6
- 376866 Heracleum lehmannianum: 10.1007/BF00570685
- 473995 Heracleum yungningense: 10.1248/CPB.53.701
- 681474 Picramnia latifolia:
- 1129486 Picramnia antidesma:
- 2686320 Picramnia teapensis:
- 2686326 Picramnia hirsuta:
- 40949 Angelica archangelica:
- 76959 Clausena excavata:
- 159034 Clausena anisata:
- 697038 Melicope semecarpifolia:
- 37334 Citrus maxima:
- 354518 Skimmia laureola: 10.1016/S0031-9422(00)81759-8
- 357848 Angelica genuflexa: 10.1016/0031-9422(73)85135-0
- 2004884 Vachellia flava: 10.1016/J.JEP.2007.05.015
- 1179190 Acacia ehrenbergiana: 10.1016/J.JEP.2007.05.015
- 178647 Arracacia tolucensis: 10.1016/J.JEP.2007.05.015
- 1585706 Prangos lophoptera: 10.1007/BF00563983
- 226895 Morus cathayana:
- 103973 Juniperus drupacea: 10.1016/0031-9422(73)80593-X
- 489417 Tordylium apulum:
- 354530 Zanthoxylum schinifolium:
- 697043 Zanthoxylum wutaiense: 10.1021/NP700719E
- 357845 Angelica anomala: 10.1248/YAKUSHI1947.87.9_1118
- 52471 Ferula assa-foetida: 10.1021/NP900158F
- 178713 Pteryxia terebinthina: 10.1021/NP50001A008
- 229049 Morus mongolica: 10.3987/COM-88-4771
- 56060 Butea monosperma: 10.3987/COM-11-12275
- 50182 Juniperus chinensis: 10.1016/0031-9422(92)83753-L
- 86306 Artemisia abrotanum: 10.1055/S-2006-958106
- 176616 Ageratina adenophora: 10.1002/CHIN.200731148
- 1745138 Pseudobrickellia angustissima: 10.1016/S0031-9422(00)81599-X
- 1227615 Artemisia alba: 10.1016/S0031-9422(00)81695-7
- 3498 Morus alba: 10.1248/CPB.49.151
- 984807 Dorstenia excentrica: 10.1016/S0031-9422(98)00520-2
- 984813 Dorstenia lindeniana: 10.1016/S0031-9422(98)00520-2
- 452780 Haplophyllum patavinum: 10.1016/S0031-9422(98)00356-2
- 92052 Ferula kokanica: 10.1007/BF00579439
- 52470 Ferula: 10.1021/NP0600954.S001
- 371338 Ferula diversivittata:
- 555415 Ferula szowitziana:
- 1514040 Ferula persica: 10.1007/BF00563961
- 40922 Anethum graveolens: 10.1007/BF00595084
- 371364 Ferula litwinowiana: 10.1007/BF00574600
- 1514025 Ferula iliensis: 10.1007/BF01134634
- 238942 Saussurea hieracioides: 10.1007/S10600-010-9659-5
- 238956 Saussurea superba: 10.1007/S10600-010-9659-5
- 159030 Murraya koenigii: 10.1016/J.PHYTOCHEM.2004.12.030
- 159029 Murraya siamensis: 10.1016/J.PHYTOCHEM.2004.12.030
- 13415 Chamaecyparis obtusa: 10.1248/CPB.56.60
- 984796 Dorstenia brasiliensis:
- 49840 Sophora flavescens:
- 266085 Ruta montana: 10.1016/S0031-9422(99)00486-0
- 159037 Clausena lansium: 10.1016/J.PHYTOL.2011.08.013
- 237573 Citrus sulcata: 10.1248/CPB.39.2509
- 72332 Artemisia absinthium:
- 239644 Halosciastrum melanotilingia: 10.1248/CPB.22.957
- 52491 Angelica decursiva: 10.1248/CPB.22.957
- 381990 Diplostephium ericoides: 10.1016/0031-9422(91)83038-M
- 375289 Biebersteinia heterostemon: 10.1016/S0031-9422(00)00355-1
- 74351 Biebersteinia orphanidis: 10.1016/S0031-9422(00)00355-1
- 337186 Physochlaina physaloides: 10.1007/BF00597591
- 496630 Hyalis argentea: 10.1016/S0031-9422(96)00517-1
- 488171 Citrus hassaku: 10.1271/BBB.56.1257
- 1477590 Daphne genkwa: 10.1248/YAKUSHI1947.107.7_525
- 482569 Nassauvia aculeata:
- 540063 Gypothamnium pinifolium: 10.1016/0031-9422(88)80695-2
- 714512 Uncaria hirsuta: 10.1002/JCCS.199400031
- 130303 Triptilion spinosum: 10.1016/0031-9422(88)80039-6
- 371367 Ferula microloba: 10.1007/BF00575163
- 371349 Ferula gummosa: 10.1007/BF00629773
- 401941 Artemisia xanthochroa: 10.1016/0031-9422(90)85307-2
- 76974 Atalantia buxifolia:
- 155764 Eucalyptus viminalis: 10.1007/S10600-009-9388-9
- 452790 Ruta chalepensis: 10.1021/NP000012Y
- 178675 Harbouria trachypleura: 10.1016/S0040-4039(01)01355-7
- 1226103 Philotheca fitzgeraldii: 10.1016/0031-9422(95)00382-H
- 55635 Inula helenium: 10.1007/BF00564986
- 159026 Atalantia racemosa:
- 200540 Naringi crenulata: 10.1016/S0031-9422(00)82233-5
- 4045 Apium graveolens: 10.1016/S0031-9422(98)00650-5
- 4041 Pastinaca sativa: 10.1002/CHIN.200047207
- 210365 Skimmia japonica: 10.1055/S-2006-962141
- 3908 Vicia sativa: 10.1007/BF00598366
- 4043 Petroselinum crispum: 10.1104/PP.104.1.67
- 452763 Boenninghausenia albiflora:
- 47643 Caragana frutex: 10.1007/BF00575186
- 48119 Glehnia littoralis: 10.5012/JKCS.2010.54.6.701
- 1174972 Allium rotundum: 10.1007/S10600-009-9246-9
- 4097 Nicotiana tabacum: 10.1515/ZNC-1986-11-1215
- 4113 Solanum tuberosum: 10.1016/J.PHYTOCHEM.2016.12.003
- 1500521 Parasenecio hastatus: 10.1007/S10600-005-0219-3
- 37690 Citrus trifoliata:
- 57926 Potentilla anserina: 10.1007/BF00629945
- 654633 Potentilla argentea: 10.1007/BF00629945
- 329772 Solanum dasyphyllum: 10.1021/NP50037A033
- 537489 Rhinacanthus nasutus: 10.1016/0031-9422(95)00427-9
- 555418 Ferula kirialovii: 10.1007/BF00598697
- 555413 Ferula moschata: 10.1007/BF00598697
- 595347 Leontopodium nanum: 10.1002/JCCS.200200040
- 1514035 Ferula marmarica: 10.21608/BFSA.1995.69668
- 129201 Ipomoea cairica: 10.1590/S0103-50531997000300009
- 152286 Hydrangea febrifuga: 10.1248/YAKUSHI1947.111.6_299
- 82096 Eleutherococcus senticosus: 10.1016/B978-1-4377-2333-5.00087-0
- 1224753 Clausena anisum-olens: 10.1271/BBB.100143
- 3827 Cicer arietinum: 10.1007/BF00630191
- 1585704 Prangos latiloba: 10.1007/BF00570862
- 2259079 Polygonatum orientale: 10.1007/S10600-011-0068-1
- 1623365 Deutzia hookeriana: 10.1016/0031-9422(91)85150-X
- 984477 Deutzia corymbosa: 10.1016/0031-9422(91)85150-X
- 265785 Atractylodes macrocephala:
- 171767 Chuquiraga ulicina: 10.4067/S0366-16442000000100007
- 67938 Zanthoxylum armatum: 10.1007/978-3-642-71425-2_1
- 49562 Peucedanum: 10.1055/S-2003-38876
- 1504338 Poa huecu: 10.1016/S0031-9422(00)83142-8
- 45385 Aloe arborescens: 10.1007/S10600-009-9405-Z
- 1902363 Peddiea fischeri: 10.1021/NP50026A020
- 254913 Saussurea laniceps: 10.1007/SPRINGERREFERENCE_69384
- 401925 Artemisia palustris: 10.1007/BF00713338
- 491195 Semenovia dasycarpa:
- 510746 Crataegus flava: 10.1016/S0367-326X(01)00315-X
- 82086 Eryngium campestre: 10.1016/0031-9422(86)88036-0
- 159070 Triphasia trifolia: 10.1016/0031-9422(81)85288-0
- 1027791 Artemisia ordosica: 10.1007/S11418-009-0385-X
- 81513 Pterocaulon: 10.1016/J.EJMECH.2012.09.007
- 1542382 Chaptalia integerrima: 10.1016/S0305-1978(00)00110-1
- 452786 Haplophyllum villosum: 10.3390/MOLECULES16032268
- 401905 Artemisia jacutica: 10.1007/BF00629808
- 72341 Artemisia dracunculus: 10.1007/BF00629809
- 637481 Artemisia keiskeana: 10.1007/BF00574599
- 4220 Artemisia vulgaris: 10.1007/BF00574599
- 43364 Aesculus hippocastanum: 10.1201/B10413-17
- 3760 Prunus persica: 10.1007/BF00579835
- 39358 Prunella vulgaris: 10.1007/BF00579835
- 1620273 Brosimum gaudichaudii: 10.1021/NP50093A015
- 1911 Streptomyces griseus: 10.1128/AEM.46.2.468-474.1983
- 68535 Casimiroa edulis: 10.1002/PTR.3690
- 29786 Cruciata laevipes: 10.1007/BF00568231
- 715653 Cruciata taurica: 10.1007/BF00568231
- 51276 Bidens tripartita: 10.1007/BF00564344
- 41522 Centaurea cyanus: 10.1007/BF00630089
- 145517 Centaurea scabiosa: 10.1007/BF00630089
- 1486575 Centaurea pseudomaculosa: 10.1007/BF00630089
- 347529 Centaurea solstitialis: 10.1007/BF00630089
- 5158 Ceratocystis fimbriata: 10.1016/0031-9422(91)80014-R
- 49605 Rhododendron groenlandicum: 10.1002/CHIN.200322269
- 75587 Rhododendron diversipilosum: 10.1002/CHIN.200322269
- 2051890 Rhododendron tolmachevii: 10.1002/CHIN.200322269
- 49170 Rhododendron tomentosum: 10.1002/CHIN.200322269
- 313328 Rhododendron hypoleucum: 10.1002/CHIN.200322269
- 271192 Pimpinella anisum: 10.1055/S-2006-959644
- 48109 Cicuta virosa: 10.1007/BF00580908
- 630317 Helichrysum maracandicum: 10.1007/BF00598091
- 282722 Achillea biebersteinii: 10.1007/BF00579153
- 57940 Potentilla erecta: 10.1007/BF00598776
- 41496 Calendula officinalis: 10.1007/BF00598365
- 261776 Helichrysum arenarium: 10.1007/BF00598365
- 382038 Parastrephia quadrangularis: 10.1016/S0031-9422(00)82580-7
- 371390 Ferula tadshikorum: 10.1007/BF00575772
- 39416 Tuber melanosporum: 10.1016/S0031-9422(96)00451-7
- 1514018 Ferula gigantea: 10.1007/BF00565039
- 47082 Melilotus albus: 10.1002/JSFA.2740151101
- 371376 Ferula ovina: 10.1007/BF00567695
- 1514030 Ferula kopetdagensis: 10.1007/BF00567695
- 1224771 Micromelum integerrimum: 10.4038/JNSFSR.V11I1.8409
- 159056 Micromelum ceylanicum: 10.4038/JNSFSR.V11I1.8409
- 170040 Breonadia salicina: 10.1016/0031-9422(73)80702-2
- 4442 Camellia sinensis: 10.1007/BF00568233
- 1903227 Artemisia scotina: 10.1007/BF00564342
- 2831626 Angelica pachycarpa: 10.1007/BF01926538
- 9606 Homo sapiens:
- 142738 Stellera chamaejasme:
- 68554 Phellodendron amurense:
- 159071 Zanthoxylum ailanthoides:
- 76967 Glycosmis pentaphylla:
- 43711 Murraya paniculata:
- 2901850 Murraya exotica:
- 354522 Tetradium glabrifolium:
- 880079 Rhododendron dauricum: 10.1007/S10600-010-9649-7
- 354509 Phellodendron chinense var. glabriusculum: 10.1021/NP030034V
- 697203 Phellodendron amurense var. wilsonii: 10.1021/NP030034V
- 2099548 Zanthoxylum zanthoxyloides: 10.1021/NP50046A035
- 98504 Matricaria chamomilla:
- 115623 Herniaria: 10.1007/BF00566073
- 3039 Euglena gracilis: 10.3389/FBIOE.2021.662655
- 1227633 Artemisia minor:
- 237931 Viburnum cylindricum: 10.1002/HLCA.200800420
- 669127 Artemisia lactiflora: 10.4268/CJCMM20141334
- 1056465 Zanthoxylum beecheyanum: 10.1002/JCCS.200400159
- 216479 Euphorbia maculata: 10.4268/CJCMM20141227
- 216481 Euphorbia nutans: 10.4268/CJCMM20141227
- 29760 Vitis vinifera: 10.1002/JSSC.200500003
- 53873 Dipteryx odorata: 10.1021/JF00111A051
- 4047 Coriandrum sativum: 10.1016/0031-9422(95)00930-2
- 97171 Abies nephrolepis: 10.1002/CBDV.201000373
- 210328 Maclura tricuspidata: 10.3987/COM-90-5416
- 1435564 Kalanchoe laciniata: 10.1021/NP50065A009
- 1091133 Astragalus onobrychis: 10.1007/BF00630446
- 203000 Rhodiola sacra: 10.1007/BF00564830
- 237933 Viburnum dilatatum: 10.1016/0031-9422(95)00790-3
- 1264805 Astragalus brachycarpus: 10.1007/BF00564977
- 100580 Ficus virens: 10.1016/J.JEP.2008.06.025
- 3494 Ficus carica: 10.1016/J.JEP.2008.06.025
- 549434 Zanthoxylum rhoifolium:
- 1968 Streptomyces cellulosae: 10.1186/S12906-018-2154-4
- 46147 Portulaca oleracea: 10.1002/HLCA.201000250
- 125587 Bistorta officinalis: 10.4268/CJCMM20161721
- 254780 Persicaria amphibia: 10.4268/CJCMM20161721
- 157791 Vigna radiata: 10.1007/BF00598601
- 3916 Vigna radiata var. radiata: 10.1007/BF00598601
- 3885 Phaseolus vulgaris:
- 53861 Securigera varia:
- 181251 Securigera elegans:
- 390705 Securigera securidaca: 10.1007/BF00598775
- 203004 Rhodiola heterodonta: 10.1007/BF00564822
- 1279044 Melilotus messanensis: 10.1055/S-0028-1097913
- 200951 Melilotus indicus: 10.1055/S-0028-1097913
- 195662 Prunus prostrata: 10.1021/NP50102A017
- 428217 Callisia fragrans: 10.1007/S10600-009-9174-8
- 212301 Euphorbia humifusa: 10.1016/J.BMCL.2014.03.014
- 91096 Hylotelephium ewersii: 10.1007/BF00567817
- 2816892 Heteroplexis microcephala: 10.1021/NP900213W
- 35883 Ipomoea nil:
- 487764 Rhodiola quadrifida: 10.1007/BF00563908
- 1442767 Rhodiola coccinea: 10.1007/BF00563908
- 182159 Rhododendron spinuliferum: 10.1007/S10600-009-9410-2
- 626692 Caragana spinosa: 10.1007/S10600-012-0124-5
- 72349 Artemisia nova: 10.1016/S0021-9673(01)97678-2
- 55611 Artemisia tridentata:
- 187461 Chamaecyparis formosensis: 10.1016/S0031-9422(99)00074-6
- 1441046 Lomatia hirsuta: 10.1016/S0378-8741(97)00048-2
- 4222 Carthamus tinctorius: 10.1023/B:CONC.0000025456.09089.84
- 85712 Angelica gigas:
- 48101 Angelica dahurica:
- 357970 Angelica biserrata:
- 312530 Angelica pubescens:
- 369397 Picea neoveitchii: 10.1016/J.PHYTOCHEM.2011.01.018
- 33117 Mandragora officinarum: 10.1016/J.PHYTOCHEM.2005.07.016
- 389206 Mandragora autumnalis: 10.1016/J.PHYTOCHEM.2005.07.016
- 100573 Ficus septica: 10.3987/COM-02-9615
- 1745051 Disynaphia multicrenulata: 10.1016/S0031-9422(00)80481-1
- 573714 Baccharis trinervis: 10.1016/S0031-9422(00)80758-X
- 354517 Skimmia reevesiana: 10.1016/S0031-9422(00)84814-1
- 23278 Vahlia capensis: 10.1016/0031-9422(94)00710-B
- 1227617 Artemisia assoana: 10.1016/S0031-9422(00)83891-1
- 72339 Artemisia chamaemelifolia:
- 205376 Artemisia santolinifolia:
- 401898 Artemisia gmelinii:
- 392618 Cunila: 10.1007/S00299-018-2303-8
- 205371 Artemisia marschalliana: 10.1016/S0031-9422(00)88402-2
- 224035 Daphne oleoides:
- 329675 Daphne odora:
- 1619493 Melicope hayesii: 10.1016/S0031-9422(98)00720-1
- 23110 Hydrangea macrophylla:
- 859264 Hydrangea serrata: 10.1248/CPB.40.3121
- 1811969 Artemisia vestita: 10.1055/S-1999-13965
- 2753872 Daphne acutiloba: 10.1016/S0031-9422(98)00181-2
- 66680 Daphne mezereum:
- 224084 Wikstroemia canescens: 10.1248/CPB.60.554
- 669133 Artemisia mongolica: 10.1055/S-2006-957946
- 88733 Pinus armandii:
- 2753873 Daphne feddei: 10.1080/10286020.2011.621892
- 885948 Daphne tangutica: 10.1016/J.FITOTE.2009.07.002
- 347984 Coronilla viminalis:
- 390707 Coronilla vaginalis:
- 66391 Fatoua villosa: 10.1002/CBDV.200900326
- 241879 Fatoua pilosa: 10.1002/CBDV.200900326
- 118892 Coronilla scorpioides:
- 52496 Prangos: 10.1007/BF00781092
- 48026 Ammi majus:
- 325744 Prangos uloptera: 10.1248/CPB.49.877
- 1585712 Prangos tschimganica: 10.1248/CPB.49.877
- 463862 Ficus nervosa: 10.1002/CBDV.200900227
- 282648 Asterolasia phebalioides: 10.1016/0305-1978(94)90036-1
- 1090619 Ayapana triplinervis: 10.1016/0031-9422(71)85045-8
- 171251 Citrus medica:
- 549427 Metrodorea nigra: 10.1016/0031-9422(95)00504-Z
- 265806 Angelica japonica: 10.1248/CPB.29.2565
- 142181 Edgeworthia chrysantha:
- 883867 Matricaria discoidea: 10.1007/BF00579084
- 56017 Matricaria matricarioides: 10.1007/BF00579084
- 43493 Haldina cordifolia:
- 169606 Tagetes lucida: 10.1021/JF053071W
- 401909 Artemisia laciniata: 10.1002/JLAC.198619861208
- 2567738 Yponomeuta padella: 10.1007/BF01041730
- 263927 Yponomeuta mahalebellus: 10.1007/BF01041730
- 129217 Prunus mahaleb: 10.1007/BF01041730
- 860753 Hydrangea heteromalla:
- 52833 Hydrangea paniculata:
- 498914 Hydrangea chinensis:
- 489434 Prangos ferulacea: 10.1590/S0102-695X2008000100002
- 118509 Glebionis segetum:
- 380075 Heracleum grandiflorum: 10.1007/BF02249699
- 380073 Heracleum dissectum: 10.1007/S11418-008-0266-8
- 99506 Heracleum candicans: 10.1007/S11418-008-0266-8
- 282612 Nematolepis squamea: 10.1016/0031-9422(92)83450-D
- 282620 Rhadinothamnus anceps: 10.1016/0031-9422(92)83450-D
- 282633 Phebalium squamulosum:
- 357850 Angelica keiskei: 10.1016/0031-9422(90)85357-L
- 68527 Aegle marmelos:
- 77053 Pleiospermium alatum:
- 446321 Althaea armeniaca: 10.1007/BF00630189
- 145745 Althaea officinalis: 10.1007/BF00630189
- 714449 Artemisia anomala: 10.1016/S0031-9422(00)83589-X
- 298346 Dictamnus albus:
- 217505 Sinacalia tangutica:
- 1044962 Rhododendron lepidotum: 10.1016/J.CCLET.2009.11.015
- 2715869 Daphne papyracea: 10.1248/CPB.34.595
- 2783874 Daphne mucronata:
- 202097 Scapholeberis mucronata:
- 546994 Daphne bholua: 10.1016/S0367-326X(99)00010-6
- 376866 Heracleum lehmannianum: 10.1007/BF00570685
- 473995 Heracleum yungningense: 10.1248/CPB.53.701
- 681474 Picramnia latifolia:
- 1129486 Picramnia antidesma:
- 2686320 Picramnia teapensis:
- 2686326 Picramnia hirsuta:
- 40949 Angelica archangelica:
- 76959 Clausena excavata:
- 159034 Clausena anisata:
- 697038 Melicope semecarpifolia:
- 37334 Citrus maxima:
- 354518 Skimmia laureola: 10.1016/S0031-9422(00)81759-8
- 357848 Angelica genuflexa: 10.1016/0031-9422(73)85135-0
- 2004884 Vachellia flava: 10.1016/J.JEP.2007.05.015
- 1179190 Acacia ehrenbergiana: 10.1016/J.JEP.2007.05.015
- 178647 Arracacia tolucensis: 10.1016/J.JEP.2007.05.015
- 1585706 Prangos lophoptera: 10.1007/BF00563983
- 226895 Morus cathayana:
- 103973 Juniperus drupacea: 10.1016/0031-9422(73)80593-X
- 489417 Tordylium apulum:
- 354530 Zanthoxylum schinifolium:
- 697043 Zanthoxylum wutaiense: 10.1021/NP700719E
- 357845 Angelica anomala: 10.1248/YAKUSHI1947.87.9_1118
- 52471 Ferula assa-foetida: 10.1021/NP900158F
- 178713 Pteryxia terebinthina: 10.1021/NP50001A008
- 229049 Morus mongolica: 10.3987/COM-88-4771
- 56060 Butea monosperma: 10.3987/COM-11-12275
- 50182 Juniperus chinensis: 10.1016/0031-9422(92)83753-L
- 86306 Artemisia abrotanum: 10.1055/S-2006-958106
- 176616 Ageratina adenophora: 10.1002/CHIN.200731148
- 1745138 Pseudobrickellia angustissima: 10.1016/S0031-9422(00)81599-X
- 1227615 Artemisia alba: 10.1016/S0031-9422(00)81695-7
- 3498 Morus alba: 10.1248/CPB.49.151
- 984807 Dorstenia excentrica: 10.1016/S0031-9422(98)00520-2
- 984813 Dorstenia lindeniana: 10.1016/S0031-9422(98)00520-2
- 452780 Haplophyllum patavinum: 10.1016/S0031-9422(98)00356-2
- 92052 Ferula kokanica: 10.1007/BF00579439
- 52470 Ferula: 10.1021/NP0600954.S001
- 371338 Ferula diversivittata:
- 555415 Ferula szowitziana:
- 1514040 Ferula persica: 10.1007/BF00563961
- 40922 Anethum graveolens: 10.1007/BF00595084
- 371364 Ferula litwinowiana: 10.1007/BF00574600
- 1514025 Ferula iliensis: 10.1007/BF01134634
- 238942 Saussurea hieracioides: 10.1007/S10600-010-9659-5
- 238956 Saussurea superba: 10.1007/S10600-010-9659-5
- 159030 Murraya koenigii: 10.1016/J.PHYTOCHEM.2004.12.030
- 159029 Murraya siamensis: 10.1016/J.PHYTOCHEM.2004.12.030
- 13415 Chamaecyparis obtusa: 10.1248/CPB.56.60
- 984796 Dorstenia brasiliensis:
- 49840 Sophora flavescens:
- 266085 Ruta montana: 10.1016/S0031-9422(99)00486-0
- 159037 Clausena lansium: 10.1016/J.PHYTOL.2011.08.013
- 237573 Citrus sulcata: 10.1248/CPB.39.2509
- 72332 Artemisia absinthium:
- 239644 Halosciastrum melanotilingia: 10.1248/CPB.22.957
- 52491 Angelica decursiva: 10.1248/CPB.22.957
- 381990 Diplostephium ericoides: 10.1016/0031-9422(91)83038-M
- 375289 Biebersteinia heterostemon: 10.1016/S0031-9422(00)00355-1
- 74351 Biebersteinia orphanidis: 10.1016/S0031-9422(00)00355-1
- 337186 Physochlaina physaloides: 10.1007/BF00597591
- 496630 Hyalis argentea: 10.1016/S0031-9422(96)00517-1
- 488171 Citrus hassaku: 10.1271/BBB.56.1257
- 1477590 Daphne genkwa: 10.1248/YAKUSHI1947.107.7_525
- 482569 Nassauvia aculeata:
- 540063 Gypothamnium pinifolium: 10.1016/0031-9422(88)80695-2
- 714512 Uncaria hirsuta: 10.1002/JCCS.199400031
- 130303 Triptilion spinosum: 10.1016/0031-9422(88)80039-6
- 371367 Ferula microloba: 10.1007/BF00575163
- 371349 Ferula gummosa: 10.1007/BF00629773
- 401941 Artemisia xanthochroa: 10.1016/0031-9422(90)85307-2
- 76974 Atalantia buxifolia:
- 155764 Eucalyptus viminalis: 10.1007/S10600-009-9388-9
- 452790 Ruta chalepensis: 10.1021/NP000012Y
- 178675 Harbouria trachypleura: 10.1016/S0040-4039(01)01355-7
- 1226103 Philotheca fitzgeraldii: 10.1016/0031-9422(95)00382-H
- 55635 Inula helenium: 10.1007/BF00564986
- 159026 Atalantia racemosa:
- 200540 Naringi crenulata: 10.1016/S0031-9422(00)82233-5
- 4045 Apium graveolens: 10.1016/S0031-9422(98)00650-5
- 4041 Pastinaca sativa: 10.1002/CHIN.200047207
- 210365 Skimmia japonica: 10.1055/S-2006-962141
- 3908 Vicia sativa: 10.1007/BF00598366
- 4043 Petroselinum crispum: 10.1104/PP.104.1.67
- 452763 Boenninghausenia albiflora:
- 47643 Caragana frutex: 10.1007/BF00575186
- 48119 Glehnia littoralis: 10.5012/JKCS.2010.54.6.701
- 1174972 Allium rotundum: 10.1007/S10600-009-9246-9
- 4097 Nicotiana tabacum: 10.1515/ZNC-1986-11-1215
- 4113 Solanum tuberosum: 10.1016/J.PHYTOCHEM.2016.12.003
- 1500521 Parasenecio hastatus: 10.1007/S10600-005-0219-3
- 37690 Citrus trifoliata:
- 57926 Potentilla anserina: 10.1007/BF00629945
- 654633 Potentilla argentea: 10.1007/BF00629945
- 329772 Solanum dasyphyllum: 10.1021/NP50037A033
- 537489 Rhinacanthus nasutus: 10.1016/0031-9422(95)00427-9
- 555418 Ferula kirialovii: 10.1007/BF00598697
- 555413 Ferula moschata: 10.1007/BF00598697
- 595347 Leontopodium nanum: 10.1002/JCCS.200200040
- 1514035 Ferula marmarica: 10.21608/BFSA.1995.69668
- 129201 Ipomoea cairica: 10.1590/S0103-50531997000300009
- 152286 Hydrangea febrifuga: 10.1248/YAKUSHI1947.111.6_299
- 82096 Eleutherococcus senticosus: 10.1016/B978-1-4377-2333-5.00087-0
- 1224753 Clausena anisum-olens: 10.1271/BBB.100143
- 3827 Cicer arietinum: 10.1007/BF00630191
- 1585704 Prangos latiloba: 10.1007/BF00570862
- 2259079 Polygonatum orientale: 10.1007/S10600-011-0068-1
- 1623365 Deutzia hookeriana: 10.1016/0031-9422(91)85150-X
- 984477 Deutzia corymbosa: 10.1016/0031-9422(91)85150-X
- 265785 Atractylodes macrocephala:
- 171767 Chuquiraga ulicina: 10.4067/S0366-16442000000100007
- 67938 Zanthoxylum armatum: 10.1007/978-3-642-71425-2_1
- 49562 Peucedanum: 10.1055/S-2003-38876
- 1504338 Poa huecu: 10.1016/S0031-9422(00)83142-8
- 45385 Aloe arborescens: 10.1007/S10600-009-9405-Z
- 1902363 Peddiea fischeri: 10.1021/NP50026A020
- 254913 Saussurea laniceps: 10.1007/SPRINGERREFERENCE_69384
- 401925 Artemisia palustris: 10.1007/BF00713338
- 491195 Semenovia dasycarpa:
- 510746 Crataegus flava: 10.1016/S0367-326X(01)00315-X
- 82086 Eryngium campestre: 10.1016/0031-9422(86)88036-0
- 159070 Triphasia trifolia: 10.1016/0031-9422(81)85288-0
- 1027791 Artemisia ordosica: 10.1007/S11418-009-0385-X
- 81513 Pterocaulon: 10.1016/J.EJMECH.2012.09.007
- 1542382 Chaptalia integerrima: 10.1016/S0305-1978(00)00110-1
- 452786 Haplophyllum villosum: 10.3390/MOLECULES16032268
- 401905 Artemisia jacutica: 10.1007/BF00629808
- 72341 Artemisia dracunculus: 10.1007/BF00629809
- 637481 Artemisia keiskeana: 10.1007/BF00574599
- 4220 Artemisia vulgaris: 10.1007/BF00574599
- 43364 Aesculus hippocastanum: 10.1201/B10413-17
- 3760 Prunus persica: 10.1007/BF00579835
- 39358 Prunella vulgaris: 10.1007/BF00579835
- 1620273 Brosimum gaudichaudii: 10.1021/NP50093A015
- 1911 Streptomyces griseus: 10.1128/AEM.46.2.468-474.1983
- 68535 Casimiroa edulis: 10.1002/PTR.3690
- 29786 Cruciata laevipes: 10.1007/BF00568231
- 715653 Cruciata taurica: 10.1007/BF00568231
- 51276 Bidens tripartita: 10.1007/BF00564344
- 41522 Centaurea cyanus: 10.1007/BF00630089
- 145517 Centaurea scabiosa: 10.1007/BF00630089
- 1486575 Centaurea pseudomaculosa: 10.1007/BF00630089
- 347529 Centaurea solstitialis: 10.1007/BF00630089
- 5158 Ceratocystis fimbriata: 10.1016/0031-9422(91)80014-R
- 49605 Rhododendron groenlandicum: 10.1002/CHIN.200322269
- 75587 Rhododendron diversipilosum: 10.1002/CHIN.200322269
- 2051890 Rhododendron tolmachevii: 10.1002/CHIN.200322269
- 49170 Rhododendron tomentosum: 10.1002/CHIN.200322269
- 313328 Rhododendron hypoleucum: 10.1002/CHIN.200322269
- 271192 Pimpinella anisum: 10.1055/S-2006-959644
- 48109 Cicuta virosa: 10.1007/BF00580908
- 630317 Helichrysum maracandicum: 10.1007/BF00598091
- 282722 Achillea biebersteinii: 10.1007/BF00579153
- 57940 Potentilla erecta: 10.1007/BF00598776
- 41496 Calendula officinalis: 10.1007/BF00598365
- 261776 Helichrysum arenarium: 10.1007/BF00598365
- 382038 Parastrephia quadrangularis: 10.1016/S0031-9422(00)82580-7
- 371390 Ferula tadshikorum: 10.1007/BF00575772
- 39416 Tuber melanosporum: 10.1016/S0031-9422(96)00451-7
- 1514018 Ferula gigantea: 10.1007/BF00565039
- 47082 Melilotus albus: 10.1002/JSFA.2740151101
- 371376 Ferula ovina: 10.1007/BF00567695
- 1514030 Ferula kopetdagensis: 10.1007/BF00567695
- 1224771 Micromelum integerrimum: 10.4038/JNSFSR.V11I1.8409
- 159056 Micromelum ceylanicum: 10.4038/JNSFSR.V11I1.8409
- 170040 Breonadia salicina: 10.1016/0031-9422(73)80702-2
- 4442 Camellia sinensis: 10.1007/BF00568233
- 1903227 Artemisia scotina: 10.1007/BF00564342
- 2831626 Angelica pachycarpa: 10.1007/BF01926538
- 9606 Homo sapiens: -
- 205692 Forsythia koreana: 10.1016/S0031-9422(00)83456-1
- 205692 Forsythia koreana: 10.1016/S0031-9422(97)01134-5
- 205691 Forsythia viridissima: 10.1016/S0031-9422(00)83456-1
- 205691 Forsythia viridissima: 10.1016/S0031-9422(97)01134-5
- 126358 Abeliophyllum distichum: 10.1016/S0031-9422(97)01134-5
- 363423 Centaurea deflexa: 10.1016/J.EJMECH.2011.03.011
- 2753873 Daphne feddei: 10.1021/NP8004166
- 137893 Saussurea medusa: 10.1248/CPB.53.1416
- 137893 Saussurea medusa: 10.1016/S0304-3835(00)00499-7
- 137893 Saussurea medusa: 10.1016/S0031-9422(01)00429-0
- 205694 Forsythia ovata: 10.1248/CPB.36.3667
- 1486496 Centaurea arenaria: 10.1002/PTR.3187
- 2893703 Saussurea macrota: 10.1002/CHIN.200516160
- 196747 Onopordum acaulon: 10.1016/0031-9422(92)83742-H
- 297478 Onopordum illyricum: 10.1021/NP990098Z
- 254913 Saussurea laniceps: 10.1016/S1875-5364(11)60016-2
- 254913 Saussurea laniceps: 10.1002/HLCA.200790096
- 276781 Trachelospermum asiaticum: 10.1016/0031-9422(72)80115-8
- 276781 Trachelospermum asiaticum: 10.1248/CPB.34.4340
- 373155 Gaillardia aestivalis: 10.1016/S0031-9422(00)95216-6
- 75648 Centaurea imperialis: 10.1016/0031-9422(81)85287-9
- 200489 Saussurea involucrata: 10.1080/10286020.2010.499856
- 4217 Arctium lappa: 10.1248/CPB.44.2300
- 4217 Arctium lappa: 10.1248/BPB.19.1515
- 4217 Arctium lappa: 10.1016/S0031-9422(00)89550-3
- 4217 Arctium lappa: 10.1007/978-1-4613-1855-2_22
- 4217 Arctium lappa: 10.1016/J.PHYMED.2009.04.005
- 4217 Arctium lappa: 10.1007/978-3-540-71095-0_1382
- 4217 Arctium lappa: 10.1016/J.JPBA.2009.03.018
- 429296 Trachelospermum axillare: 10.1016/0031-9422(93)85183-R
- 126418 Forsythia suspensa: 10.1002/RCM.2875
- 947960 Trachelospermum gracilipes: 10.1016/0031-9422(72)80115-8
- 50189 Torreya nucifera: 10.1055/S-2001-15804
- 41536 Centaurea melitensis: 10.1016/J.PHYTOCHEM.2006.08.012
- 41536 Centaurea melitensis: 10.1016/S0305-1978(01)00062-X
- 41506 Plectocephalus americanus: 10.1016/J.PHYTOCHEM.2006.08.012
- 41506 Plectocephalus americanus: 10.1016/S0305-1978(01)00062-X
- 446849 Saussurea salicifolia: 10.1016/J.FCT.2010.05.056
- 75633 Centaurea nigra: 10.1016/S0305-1978(02)00227-2
- 363450 Centaurea sclerolepis: 10.1177/1934578X0600100403
- 145513 Centaurea raphanina: 10.1590/S0102-695X2007000200003
- 69389 Trachelospermum jasminoides: 10.1248/YAKUSHI1947.93.4_539
- 276781 Trachelospermum asiaticum: 10.1248/YAKUSHI1947.93.4_539
- 569774 金线莲: -
- 7091 Bombyx Mori L.: -
- 41496 Calendula Officinalis: -
- 3625 Actinidia Chinensis Planch: -
- 259893 Artemisia argyi Lévl.et Vant.: -
- 48101 Angelica dahurica ( Fisch.ex Hoffm. ) Benth. et Hook.f.: -
- 48101 Angelica dahurica (Fisch.ex Hoffm.)Benth .et Hook.f.var.formosana(Boiss.)Shsn et Yuan: -
- 165353 Angelica sinensis (Oliv.)Diels: -
- 33113 Atropa belladonna L.: -
- 312530 Angelica pubescens Maxim.f. biserata Shan et Yuan: -
- 526193 Euphorbia ebracteolata Hayata: -
- 880079 Rhododendron dauricum L.: -
- 4039 Daucus carota L.: -
- 3498 Morus alba L.: -
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Yuanyuan Chen, Xikun Liu, Jie Ma, Weida Wang, Zhaojun Li, Haijie Wu, Zhanxi Lu, Dongming Zhang, Xiaoying Zhang, Yu Zhang, Sen Zhang. Hydrangea paniculata coumarins alleviate adriamycin-induced renal lipotoxicity through activating AMPK and inhibiting C/EBPβ.
Journal of ethnopharmacology.
2024 Jul; 329(?):118156. doi:
10.1016/j.jep.2024.118156
. [PMID: 38583729] - Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products.
ACS pharmacology & translational science.
2023 May; 6(5):683-701. doi:
10.1021/acsptsci.2c00194
. [PMID: 37200814] - Tong Jin, Cheng Chen. Umbelliferone delays the progression of diabetic nephropathy by inhibiting ferroptosis through activation of the Nrf-2/HO-1 pathway.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
2022 May; 163(?):112892. doi:
10.1016/j.fct.2022.112892
. [PMID: 35278496] - Mohamed A M Allam, Akef A Khowailed, Samah Elattar, Ayman M Mahmoud. Umbelliferone ameliorates oxidative stress and testicular injury, improves steroidogenesis and upregulates peroxisome proliferator-activated receptor gamma in type 2 diabetic rats.
The Journal of pharmacy and pharmacology.
2022 Apr; 74(4):573-584. doi:
10.1093/jpp/rgab083
. [PMID: 34156072] - Mirosław Zagaja, Anna Zagaja, Joanna Szala-Rycaj, Aleksandra Szewczyk, Marta Kinga Lemieszek, Grzegorz Raszewski, Marta Andres-Mach. Influence of Umbelliferone on the Anticonvulsant and Neuroprotective Activity of Selected Antiepileptic Drugs: An In Vivo and In Vitro Study.
International journal of molecular sciences.
2022 Mar; 23(7):. doi:
10.3390/ijms23073492
. [PMID: 35408852] - Zongmei Wu, Yana Geng, Manon Buist-Homan, Han Moshage. Scopoletin and umbelliferone protect hepatocytes against palmitate- and bile acid-induced cell death by reducing endoplasmic reticulum stress and oxidative stress.
Toxicology and applied pharmacology.
2022 02; 436(?):115858. doi:
10.1016/j.taap.2021.115858
. [PMID: 34979142] - Jian-Wei Zhang, Yuan Xiong, Feng Wang, Fu-Mao Zhang, Xiaodi Yang, Guo-Qiang Lin, Ping Tian, Guangbo Ge, Dingding Gao. Discovery of 9,10-dihydrophenanthrene derivatives as SARS-CoV-2 3CLpro inhibitors for treating COVID-19.
European journal of medicinal chemistry.
2022 Jan; 228(?):114030. doi:
10.1016/j.ejmech.2021.114030
. [PMID: 34883292] - Tajpreet Kaur, Damanpreet Singh, Devendra Pathak, Amrit P Singh, Balbir Singh. Umbelliferone attenuates glycerol-induced myoglobinuric acute kidney injury through peroxisome proliferator-activated receptor-γ agonism in rats.
Journal of biochemical and molecular toxicology.
2021 Nov; 35(11):e22892. doi:
10.1002/jbt.22892
. [PMID: 34409680] - Xuezhe Piao, Hee Sun Byun, So-Ra Lee, Eunjin Ju, Kyeong Ah Park, Kyung-Cheol Sohn, Khong Trong Quan, Jinbae Lee, MinKyun Na, Gang Min Hur. 8-Geranylumbelliferone isolated from Paramignya trimera triggers RIPK1/RIPK3-dependent programmed cell death upon TNFR1 ligation.
Biochemical pharmacology.
2021 10; 192(?):114733. doi:
10.1016/j.bcp.2021.114733
. [PMID: 34411570] - Fares E M Ali, Emad H M Hassanein, Ali H El-Bahrawy, Zainab M M Omar, Eman K Rashwan, Basil A Abdel-Wahab, Tarek H Abd-Elhamid. Nephroprotective effect of umbelliferone against cisplatin-induced kidney damage is mediated by regulation of NRF2, cytoglobin, SIRT1/FOXO-3, and NF- kB-p65 signaling pathways.
Journal of biochemical and molecular toxicology.
2021 May; 35(5):e22738. doi:
10.1002/jbt.22738
. [PMID: 33522649] - Peng-Chao Huo, Xiao-Qing Guan, Peng Liu, Yun-Qing Song, Meng-Ru Sun, Rong-Jing He, Li-Wei Zou, Li-Juan Xue, Jin-Hui Shi, Nan Zhang, Zhi-Guo Liu, Guang-Bo Ge. Design, synthesis and biological evaluation of indanone-chalcone hybrids as potent and selective hCES2A inhibitors.
European journal of medicinal chemistry.
2021 Jan; 209(?):112856. doi:
10.1016/j.ejmech.2020.112856
. [PMID: 33007602] - Peng-Chao Huo, Qing Hu, Sheng Shu, Qi-Hang Zhou, Rong-Jing He, Jie Hou, Xiao-Qing Guan, Dong-Zhu Tu, Xu-Dong Hou, Peng Liu, Nan Zhang, Zhi-Guo Liu, Guang-Bo Ge. Design, synthesis and biological evaluation of novel chalcone-like compounds as potent and reversible pancreatic lipase inhibitors.
Bioorganic & medicinal chemistry.
2021 01; 29(?):115853. doi:
10.1016/j.bmc.2020.115853
. [PMID: 33214035] - Yang-Liu Xia, Jing-Jing Wang, Shi-Yang Li, Yong Liu, Frank J Gonzalez, Ping Wang, Guang-Bo Ge. Synthesis and structure-activity relationship of coumarins as potent Mcl-1 inhibitors for cancer treatment.
Bioorganic & medicinal chemistry.
2021 01; 29(?):115851. doi:
10.1016/j.bmc.2020.115851
. [PMID: 33218896] - Joanna Sumorek-Wiadro, Adrian Zając, Ewa Langner, Krystyna Skalicka-Woźniak, Aleksandra Maciejczyk, Wojciech Rzeski, Joanna Jakubowicz-Gil. Antiglioma Potential of Coumarins Combined with Sorafenib.
Molecules (Basel, Switzerland).
2020 Nov; 25(21):. doi:
10.3390/molecules25215192
. [PMID: 33171577] - Jae-Sung Park, Beomkoo Chung, Won-Hee Lee, Jayho Lee, Youngbae Suh, Dong-Chan Oh, Ki-Bong Oh, Jongheon Shin. Sortase A-Inhibitory Coumarins from the Folk Medicinal Plant Poncirus trifoliata.
Journal of natural products.
2020 10; 83(10):3004-3011. doi:
10.1021/acs.jnatprod.0c00551
. [PMID: 32996318] - Merhan O Hindam, Rabab H Sayed, Krystyna Skalicka-Woźniak, Barbara Budzyńska, Nesrine S El Sayed. Xanthotoxin and umbelliferone attenuate cognitive dysfunction in a streptozotocin-induced rat model of sporadic Alzheimer's disease: The role of JAK2/STAT3 and Nrf2/HO-1 signalling pathway modulation.
Phytotherapy research : PTR.
2020 Sep; 34(9):2351-2365. doi:
10.1002/ptr.6686
. [PMID: 32250498] - Rubén Seoane-Rivero, Estibaliz Ruiz-Bilbao, Rodrigo Navarro, José Manuel Laza, José María Cuevas, Beñat Artetxe, Juan M Gutiérrez-Zorrilla, José Luis Vilas-Vilela, Ángel Marcos-Fernandez. Structural Characterization of Mono and Dihydroxylated Umbelliferone Derivatives.
Molecules (Basel, Switzerland).
2020 Jul; 25(15):. doi:
10.3390/molecules25153497
. [PMID: 32751979] - Adnan Amin, Muhammad Hanif, Khizar Abbas, Muhammad Ramzan, Abdur Rasheed, Ali Zaman, Luc Pieters. Studies on effects of umbelliferon derivatives against periodontal bacteria; antibiofilm, inhibition of quorum sensing and molecular docking analysis.
Microbial pathogenesis.
2020 Jul; 144(?):104184. doi:
10.1016/j.micpath.2020.104184
. [PMID: 32304793] - Yao Fu, Xiaoxiao Tian, Lingling Han, Yilin Li, Ying Peng, Jiang Zheng. Mechanism-based inactivation of cytochrome P450 2D6 by Notopterol.
Chemico-biological interactions.
2020 May; 322(?):109053. doi:
10.1016/j.cbi.2020.109053
. [PMID: 32198085] - Wei-Feng Wu, Jia-Nan Wang, Zeng Li, Biao Wei, Juan Jin, Li Gao, Hai-Di Li, Jun Li, Hai-Yong Chen, Xiao-Ming Meng. 7-Hydroxycoumarin protects against cisplatin-induced acute kidney injury by inhibiting necroptosis and promoting Sox9-mediated tubular epithelial cell proliferation.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2020 Apr; 69(?):153202. doi:
10.1016/j.phymed.2020.153202
. [PMID: 32169782] - Xueqin Jiang, Zengjin Liu, Youzhe Yang, Hao Li, Xiaoyi Qi, Wen Xiu Ren, Mingming Deng, Muhan Lü, Jianming Wu, Sicheng Liang. A mitochondria-targeted two-photon fluorescent probe for sensing and imaging pH changes in living cells.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
2020 Jan; 224(?):117435. doi:
10.1016/j.saa.2019.117435
. [PMID: 31400745] - Mohammed F Alotaibi, Fakhria Al-Joufi, Howida S Abou Seif, Mohammed A Alzoghaibi, Laiche Djouhri, Ahmad F Ahmeda, Ayman M Mahmoud. Umbelliferone Inhibits Spermatogenic Defects and Testicular Injury in Lead-Intoxicated Rats by Suppressing Oxidative Stress and Inflammation, and Improving Nrf2/HO-1 Signaling.
Drug design, development and therapy.
2020; 14(?):4003-4019. doi:
10.2147/dddt.s265636
. [PMID: 33061305] - Tomonori Miura, Yusuke Kamiya, Shiori Hina, Yui Kobayashi, Norie Murayama, Makiko Shimizu, Hiroshi Yamazaki. Metabolic profiles of coumarin in human plasma extrapolated from a rat data set with a simplified physiologically based pharmacokinetic model.
The Journal of toxicological sciences.
2020; 45(11):695-700. doi:
10.2131/jts.45.695
. [PMID: 33132243] - Su Hui Seong, Md Yousof Ali, Hyun Ah Jung, Jae Sue Choi. Umbelliferone derivatives exert neuroprotective effects by inhibiting monoamine oxidase A, self-amyloidβ aggregation, and lipid peroxidation.
Bioorganic chemistry.
2019 11; 92(?):103293. doi:
10.1016/j.bioorg.2019.103293
. [PMID: 31557622] - Ruben Vanholme, Lisa Sundin, Keletso Carol Seetso, Hoon Kim, Xinyu Liu, Jin Li, Barbara De Meester, Lennart Hoengenaert, Geert Goeminne, Kris Morreel, Jurgen Haustraete, Huei-Hsuan Tsai, Wolfgang Schmidt, Bartel Vanholme, John Ralph, Wout Boerjan. COSY catalyses trans-cis isomerization and lactonization in the biosynthesis of coumarins.
Nature plants.
2019 10; 5(10):1066-1075. doi:
10.1038/s41477-019-0510-0
. [PMID: 31501530] - Jia-Hao Lee, Hui-Ching Mei, I-Chih Kuo, Tzong-Huei Lee, Yu-Hsin Chen, Ching-Kuo Lee. Characterizing Tyrosinase Modulators from the Roots of Angelica keiskei Using Tyrosinase Inhibition Assay and UPLC-MS/MS as the Combinatorial Novel Approach.
Molecules (Basel, Switzerland).
2019 Sep; 24(18):. doi:
10.3390/molecules24183297
. [PMID: 31510069] - Yoon Young Kang, Jihyeon Song, Jun Yeong Kim, Heesun Jung, Woon-Seok Yeo, Yoongho Lim, Hyejung Mok. Byakangelicin as a modulator for improved distribution and bioactivity of natural compounds and synthetic drugs in the brain.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2019 Sep; 62(?):152963. doi:
10.1016/j.phymed.2019.152963
. [PMID: 31128487] - Xiaoyi Qi, Tongyi Dou, Zhongqiong Wang, Jianming Wu, Ling Yang, Su Zeng, Mingming Deng, Muhan Lü, Sicheng Liang. Inhibition of human cytochrome P450 2A6 by 7-hydroxycoumarin analogues: Analysis of the structure-activity relationship and isoform selectivity.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
2019 Aug; 136(?):104944. doi:
10.1016/j.ejps.2019.05.022
. [PMID: 31163215] - Mireia Casasampere, Núria Bielsa, Daniel Riba, Laura Bassas, Ruijuan Xu, Cungui Mao, Gemma Fabriàs, José-Luis Abad, Antonio Delgado, Josefina Casas. New fluorogenic probes for neutral and alkaline ceramidases.
Journal of lipid research.
2019 06; 60(6):1174-1181. doi:
10.1194/jlr.d092759
. [PMID: 30926626] - Serena Fiorito, Federica Ianni, Francesca Preziuso, Francesco Epifano, Luca Scotti, Tonino Bucciarelli, Salvatore Genovese. UHPLC-UV/Vis Quantitative Analysis of Hydroxylated and O-prenylated Coumarins in Pomegranate Seed Extracts.
Molecules (Basel, Switzerland).
2019 May; 24(10):. doi:
10.3390/molecules24101963
. [PMID: 31121819] - Han-Qing Wang, Sha-Sha Wang, Kuok Chiufai, Qi Wang, Xiao-Lan Cheng. Umbelliferone ameliorates renal function in diabetic nephropathy rats through regulating inflammation and TLR/NF-κB pathway.
Chinese journal of natural medicines.
2019 May; 17(5):346-354. doi:
10.1016/s1875-5364(19)30040-8
. [PMID: 31171269] - Qingpeng Wang, Yan Chen, Guoshuai Li, Zhifang Liu, Jing Ma, Min Liu, Dacheng Li, Jun Han, Bingquan Wang. Synthesis and evaluation of bi-functional 7-hydroxycoumarin platinum(IV) complexes as antitumor agents.
Bioorganic & medicinal chemistry.
2019 05; 27(10):2112-2121. doi:
10.1016/j.bmc.2019.04.009
. [PMID: 30981607] - Dan Li, Zhuoliang Gu, Jingdong Zhang, Shuren Ma. Protective effect of inducible aldo-keto reductases on 4-hydroxynonenal- induced hepatotoxicity.
Chemico-biological interactions.
2019 May; 304(?):124-130. doi:
10.1016/j.cbi.2019.02.012
. [PMID: 30849339] - Zhang Sen, Wang Weida, Ma Jie, Sheng Li, Zhang Dongming, Chen Xiaoguang. Coumarin glycosides from Hydrangea paniculata slow down the progression of diabetic nephropathy by targeting Nrf2 anti-oxidation and smad2/3-mediated profibrosis.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2019 Apr; 57(?):385-395. doi:
10.1016/j.phymed.2018.12.045
. [PMID: 30849675] - Tahani Hijazin, Alzahraa Radwan, Sara Abouzeid, Gerald Dräger, Dirk Selmar. Uptake and modification of umbelliferone by various seedlings.
Phytochemistry.
2019 Jan; 157(?):194-199. doi:
10.1016/j.phytochem.2018.10.032
. [PMID: 30439620] - Liang Yang, Lintong Wu, Xiaoyuan Yao, Shiyuan Zhao, Jiao Wang, Shili Li, Wei Ding. Hydroxycoumarins: New, effective plant-derived compounds reduce Ralstonia pseudosolanacearum populations and control tobacco bacterial wilt.
Microbiological research.
2018 Oct; 215(?):15-21. doi:
10.1016/j.micres.2018.05.011
. [PMID: 30172302] - Emad H M Hassanein, Wafaa R Mohamed, Abdel-Gawad S Shalkami, Marwa M Khalaf, Ramadan A M Hemeida. Renoprotective effects of umbelliferone on methotrexate-induced renal injury through regulation of Nrf-2/Keap-1, P38MAPK/NF-κB, and apoptosis signaling pathways.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
2018 Jun; 116(Pt B):152-160. doi:
10.1016/j.fct.2018.03.041
. [PMID: 29608980] - Luca Scotti, Salvatore Genovese, Tonino Bucciarelli, Filippo Martini, Francesco Epifano, Serena Fiorito, Francesca Preziuso, Vito Alessandro Taddeo. Analysis of biologically active oxyprenylated phenylpropanoids in Tea tree oil using selective solid-phase extraction with UHPLC-PDA detection.
Journal of pharmaceutical and biomedical analysis.
2018 May; 154(?):174-179. doi:
10.1016/j.jpba.2018.03.004
. [PMID: 29549856] - Vincenzo Ferrone, Salvatore Genovese, Maura Carlucci, Matteo Tiecco, Raimondo Germani, Francesca Preziuso, Francesco Epifano, Giuseppe Carlucci, Vito Alessandro Taddeo. A green deep eutectic solvent dispersive liquid-liquid micro-extraction (DES-DLLME) for the UHPLC-PDA determination of oxyprenylated phenylpropanoids in olive, soy, peanuts, corn, and sunflower oil.
Food chemistry.
2018 Apr; 245(?):578-585. doi:
10.1016/j.foodchem.2017.10.135
. [PMID: 29287412] - Mayuresh S Garud, Yogesh A Kulkarni. Attenuation of renal damage in type I diabetic rats by umbelliferone - a coumarin derivative.
Pharmacological reports : PR.
2017 Dec; 69(6):1263-1269. doi:
10.1016/j.pharep.2017.06.014
. [PMID: 29128808] - Md Yousof Ali, Su Hui Seong, Machireddy Rajeshkumar Reddy, Sung Yong Seo, Jae Sue Choi, Hyun Ah Jung. Kinetics and Molecular Docking Studies of 6-Formyl Umbelliferone Isolated from Angelica decursiva as an Inhibitor of Cholinesterase and BACE1.
Molecules (Basel, Switzerland).
2017 Sep; 22(10):. doi:
10.3390/molecules22101604
. [PMID: 28946641] - Salvatore Genovese, Hitoshi Ashida, Yoko Yamashita, Tomoya Nakgano, Masaki Ikeda, Shirasaya Daishi, Francesco Epifano, Vito Alessandro Taddeo, Serena Fiorito. The interaction of auraptene and other oxyprenylated phenylpropanoids with glucose transporter type 4.
Phytomedicine : international journal of phytotherapy and phytopharmacology.
2017 Aug; 32(?):74-79. doi:
10.1016/j.phymed.2017.06.005
. [PMID: 28732810] - Ruijie He, Yanjun Zhang, Liangdeng Wu, Hui Nie, Yan Huang, Buming Liu, Shengping Deng, Ruiyun Yang, Shuai Huang, Zhijie Nong, Jun Li, Haiyan Chen. Benzofuran glycosides and coumarins from the bark of Streblus indicus (Bur.) Corner.
Phytochemistry.
2017 Jun; 138(?):170-177. doi:
10.1016/j.phytochem.2017.01.011
. [PMID: 28284566] - Rita de Cássia L Lima, Simone M Gramsbergen, Johannes Van Staden, Anna K Jäger, Kenneth T Kongstad, Dan Staerk. Advancing HPLC-PDA-HRMS-SPE-NMR Analysis of Coumarins in Coleonema album by Use of Orthogonal Reversed-Phase C18 and Pentafluorophenyl Separations.
Journal of natural products.
2017 04; 80(4):1020-1027. doi:
10.1021/acs.jnatprod.6b01020
. [PMID: 28248501] - Li Wang, Hai-Long Wu, Xiao-Li Yin, Yong Hu, Hui-Wen Gu, Ru-Qin Yu. Simultaneous determination of umbelliferone and scopoletin in Tibetan medicine Saussurea laniceps and traditional Chinese medicine Radix angelicae pubescentis using excitation-emission matrix fluorescence coupled with second-order calibration method.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
2017 Jan; 170(?):104-10. doi:
10.1016/j.saa.2016.07.018
. [PMID: 27423108] - Ryosuke Munakata, Alexandre Olry, Fazeelat Karamat, Vincent Courdavault, Akifumi Sugiyama, Yoshiaki Date, Célia Krieger, Prisca Silie, Emilien Foureau, Nicolas Papon, Jérémy Grosjean, Kazufumi Yazaki, Frédéric Bourgaud, Alain Hehn. Molecular evolution of parsnip (Pastinaca sativa) membrane-bound prenyltransferases for linear and/or angular furanocoumarin biosynthesis.
The New phytologist.
2016 07; 211(1):332-44. doi:
10.1111/nph.13899
. [PMID: 26918393] - Sudhakar Raja Subramaniam, Elizabeth M Ellis. Umbelliferone and esculetin protect against N-nitrosodiethylamine-induced hepatotoxicity in rats.
Cell biology international.
2016 Jul; 40(7):761-9. doi:
10.1002/cbin.10611
. [PMID: 27080985] - Govindan Sangaran Jagadeesh, Mohamed Fizur Nagoor Meeran, Palanisamy Selvaraj. Activation of β1-adrenoceptor triggers oxidative stress mediated myocardial membrane destabilization in isoproterenol induced myocardial infarcted rats: 7-hydroxycoumarin and its counter action.
European journal of pharmacology.
2016 Apr; 777(?):70-7. doi:
10.1016/j.ejphar.2016.02.063
. [PMID: 26930228] - Kristoffer Dalhoff, Michele Gottardi, Andreas Kretschmann, Nina Cedergreen. What causes the difference in synergistic potentials of propiconazole and prochloraz toward pyrethroids in Daphnia magna?.
Aquatic toxicology (Amsterdam, Netherlands).
2016 Mar; 172(?):95-102. doi:
10.1016/j.aquatox.2015.12.007
. [PMID: 26784738] - Govindan Sangaran Jagadeesh, M F Nagoor Meeran, Palanisamy Selvaraj. Protective Effects of 7-Hydroxycoumarin on Dyslipidemia and Cardiac Hypertrophy in Isoproterenol-Induced Myocardial Infarction in Rats.
Journal of biochemical and molecular toxicology.
2016 Mar; 30(3):120-7. doi:
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